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In this context, needle hydrophone measurements of the acoustic field downstream of seven rabbit tissue layers comprising skin, subcutaneous fat and muscle were performed in different geometrical configurations.
One-hundred-sixty single-fiber EMG studies of the extensor digitorum communis muscle were performed on 127 patients with myasthenia gravis; 131 demonstrated defective neuromuscular transmission.
The patient was diagnosed with poorly differentiated thyroid carcinoma, and total thyroidectomy and central node dissection with partial resection of the right recurrent nerve and esophageal muscle were performed.
SDS-extracts of muscle were performed as described [27].
Given that these regulators of the cell cycle are post-transcriptionally regulated by phosphorylation, being active within the nuclei [26] [28], immunohistochemical analyses in sections of GAS muscle were performed to discriminate nuclear and cytosolic protein expression.
Karyotyping of cultured fibroblasts and DNA extraction from patient muscle were performed according to standard protocols.
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The electrical microscopic analysis of the mitochondria of quadriceps muscle was performed by the standard method.
At 10 weeks, a biopsy of the skeletal muscle was performed for determination of insulin receptor, PPARα, and PPARγ content.
The injection of BTX-A into the masseter muscle was performed in 13-day-old rats.
Repeat BCS including part of the pectoralis major muscle was performed.
Intramuscular microdialysis in the masseter muscle was performed to sample 5-HT, glutamate, lactate, pyruvate, glucose and glycerol, and to estimate nutritive muscle blood flow.
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